A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833317



Internal ID16457186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:86152258..86341952hg38UCSC Ensembl
Outerchr16:86185864..86375558hg19UCSC Ensembl
Outerchr16:84743365..84933059hg18UCSC Ensembl
Outerchr16:84743365..84933059hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38189695
hg19189695
hg18189695
hg17189695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1452928
Samples
Known GenesLINC00917, LINC01081, LINC01082, LOC146513
MethodBAC aCGH
AnalysisExperimental SDs (SDautosome) were calculated for each experiment on the basis of the log2 ratios of the 24,392 reliable clones minus the clones removed because of low signal-to-noise ratio (SNR) or high SD of replicate clone measures (SDclone). Thresholds for determining CNV clones were set at a multiple of the SDautosome value. For each experiment, clones were annotated as uninformative if they were filtered via SNR or SDclone, as a CNV loss if the log2 ratio was less than the negative threshold, as unchanged if the log2 ratio was between the negative and positive thresholds, and as a CNV gain if the log2 ratio was above the positive threshold.
PlatformGPL2616
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833317
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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